Efficacy of a herbal formulation for PANDU NOI (Iron Deficiency Anaemia) in Children (6-12 years of age).
- Conditions
- Health Condition 1: null- Anaemic patients - 6 12 years of agePatients whose blood haemoglobin level is between 7.0 gms% ââ?¬â?? 10.9 gms%Health Condition 2: D509- Iron deficiency anemia, unspecifiedHealth Condition 3: D509- Iron deficiency anemia, unspecifiedHealth Condition 4: D509- Iron deficiency anemia, unspecified
- Registration Number
- CTRI/2017/03/008235
- Lead Sponsor
- ATIONAL INSTITUTE OF SIDDHA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria:
1.Age 6 ââ?¬â?? 12 yrs, Sex ââ?¬â?? Both male & female.
2.Patients who are willing to sign the informed consent.
3.Patients who give blood specimen for lab investigation.
4.Patients whose blood haemoglobin level is between 7.0 gms% ââ?¬â?? 10.9 gms%; MCV < 80 fl; MCHC < 34 g /dl; Serum iron concentration, 50 Ã?µg/dl & Serum Ferritin < 30 Ã?µg/L.
5.Smear which shows hypochromic microcytic anaemia.
6.Pallor of skin, mucous membrane, conjunctiva, nail beds.
7.Lassitude, Fatigue, Shortness of breath, Palpitation.
8.Anorexia, Lack of interest, Frontal headache.
Exclusion Criteria:
Based on Parental information and previous reports:
1.Congenital heart disease, Jaundice, bleeding disorders, Sickle cell Anaemia, Cancer, Renal failure.
2.Patients with chronic diseases, inherited defects.
3.Patients with infectious diseases.
Based on Laboratory investigations:
4.Smear without the appearance of hypochromic microcytic cells.
5.Any abnormality in the blood platelet count.
6.Patients who do not give blood samples for investigation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method